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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Azar — 6 UDI-DI variants, MDR (Ergoseat AS)

MD Atlas
Ergoseat AS

Data from EUDAMED, last updated May 30, 2026

Azar

709005880AZAR001CX

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Ergoseat AS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 709005880AZAR001CX
Device name: Azar
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2022

Manufacturer & authorised representative

Manufacturer

Name: Ergoseat AS
SRN: NO-MF-000012465
Country: Norway
Email: bjorn@ergoseat.no
Phone: +4747803535

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G3ZVH8VG0EVNR2BKM9ATHX0H

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

N/A07090058800069
N/A07090058800052
N/A07090058800045
N/A07090058800021
N/A07090058800038
N/A07090058800014